Ex vivo therapeutic base and prime editing using chemically derived hepatic progenitors in a mouse model of tyrosinemia type 1. Kim et al.

Published: 11 May 2021| Version 1 | DOI: 10.17632/zxxb72tkxk.1
Contributor:
Sangsu Bae

Description

Polyploid characteristics of HT1-mCdHs. (A) The ploidy distribution of HT1-mCdHs was determined using Hoechst 33342 fluorescence and FACS analysis. (B) Isolated 2c HT1-mCdHs were expanded in reprogramming medium for 14 days. The ploidy distribution of these cells shifted to 4c (3.69%) and 8c (15%) over this time period.

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